# Childrens Cetirizine Hydrochloride

NDC: 58602-856
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: Aurohealth LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, ORALLY DISINTEGRATING
Routes: ORAL
Marketing started: 20200911

FDA application: ANDA213557

## Active ingredients

- CETIRIZINE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"58602-856"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=58602-856
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cd895177-3c25-4a1b-81a0-b85f4877787a